Linked Data
ClinVar Variation Id:
67519
ClinVar RCV Id:
RCV000058248
dbSNP Id:
rs199473501
gnomAD v2:
7-150655351-C-T
gnomAD v3:
7-150958263-C-T
gnomAD v4:
7-150958263-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.150958263C>T , CM000669.2:g.150958263C>T | GRCh38 |
| NC_000007.13:g.150655351C>T , CM000669.1:g.150655351C>T | GRCh37 |
| NC_000007.12:g.150286284C>T | NCBI36 |
| NG_008916.1:g.24664G>A , LRG_288:g.24664G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000684241.1:n.1545G>A | ||
| ENST00000262186.10:c.712G>A MANE Select | ENSP00000262186.5:p.Gly238Ser | |
| ENST00000262186.9:c.712G>A | ENSP00000262186.5:p.Gly238Ser | |
| ENST00000430723.4:c.364G>A | ENSP00000387657.4:p.Gly122Ser | |
| ENST00000532957.5:n.935G>A | ||
| NM_000238.3:c.712G>A , LRG_288t1:c.712G>A | NP_000229.1:p.Gly238Ser | |
| NM_172056.2:c.712G>A , LRG_288t2:c.712G>A | NP_742053.1:p.Gly238Ser | |
| XM_011516185.1:c.412G>A | XP_011514487.1:p.Gly138Ser | |
| XM_011516186.1:c.712G>A | XP_011514488.1:p.Gly238Ser | |
| XM_011516185.2:c.412G>A | XP_011514487.1:p.Gly138Ser | |
| XM_011516186.3:c.712G>A | XP_011514488.1:p.Gly238Ser | |
| XM_017012195.1:c.562G>A | XP_016867684.1:p.Gly188Ser | |
| XM_017012196.1:c.535G>A | XP_016867685.1:p.Gly179Ser | |
| NM_000238.4:c.712G>A MANE Select | NP_000229.1:p.Gly238Ser |